Controlling cargo trafficking in multicomponent membranes
Tine Curk, Peter Wirnsberger, Jure Dobnikar, Daan Frenkel, Andela, Saric

TL;DR
This study reveals that inert membrane components with small isotropic curvatures can significantly influence cargo endocytosis and membrane trafficking, enabling cells to control these processes through membrane composition adjustments without changing receptor levels or overall curvature.
Contribution
The paper introduces a model showing how inert membrane components actively regulate cargo trafficking by affecting membrane curvature and selectivity, a novel insight into membrane dynamics.
Findings
Inert membrane components of small curvature influence endocytosis.
Membrane composition can be tuned to control cargo selectivity.
Curved lipids and proteins actively participate in trafficking regulation.
Abstract
Biological membranes typically contain a large number of different components dispersed in small concentrations in the main membrane phase, including proteins, sugars, and lipids of varying geometrical properties. Most of these components do not bind the cargo. Here, we show that such `inert' components can be crucial for precise control of cross-membrane trafficking. Using a statistical mechanics model and molecular dynamics simulations, we demonstrate that the presence of inert membrane components of small isotropic curvatures dramatically influences cargo endocytosis, even if the total spontaneous curvature of such a membrane remains unchanged. Curved lipids, such as cholesterol, as well as asymmetrically included proteins and tethered sugars can hence all be actively participating in controlling membrane trafficking of nanoscopic cargo. We find that even a low-level expression of…
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